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The influence of different helminth infection phenotypes on immune responses against HIV in co-infected adults in South Africa

BACKGROUND: The convergent distribution of the Human Immunodeficiency Virus (HIV) and helminth infections has led to the suggestion that infection with helminths exacerbates the HIV epidemic in developing countries. In South Africa, it is estimated that 57% of the population lives in poverty and car...

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Autores principales: Mkhize-Kwitshana, Zilungile L, Taylor, Myra, Jooste, Pieter, Mabaso, Musawenkosi LH, Walzl, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213674/
https://www.ncbi.nlm.nih.gov/pubmed/21999928
http://dx.doi.org/10.1186/1471-2334-11-273
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author Mkhize-Kwitshana, Zilungile L
Taylor, Myra
Jooste, Pieter
Mabaso, Musawenkosi LH
Walzl, Gerhard
author_facet Mkhize-Kwitshana, Zilungile L
Taylor, Myra
Jooste, Pieter
Mabaso, Musawenkosi LH
Walzl, Gerhard
author_sort Mkhize-Kwitshana, Zilungile L
collection PubMed
description BACKGROUND: The convergent distribution of the Human Immunodeficiency Virus (HIV) and helminth infections has led to the suggestion that infection with helminths exacerbates the HIV epidemic in developing countries. In South Africa, it is estimated that 57% of the population lives in poverty and carries the highest burden of both HIV and helmith infections, however, the disease interactions are under-researched. METHODS: We employed both coproscopy and Ascaris lumbricoides-specific serum IgE to increase diagnostic sensitivity and to distinguish between different helminth infection phenotypes and their effects on immune responses in HIV co-infected individuals. Coproscopy was done by formol ether and Kato Katz methods. HIV positive and negative adults were stratified according to the presence or absence of A. lumbricoides and/or Trichuris trichuria eggs with or without elevated Ascaris IgE. Lymphocyte subsets were phenotyped by flow cytometry. Viral loads, serum total IgE and eosinophils were also analysed. Lymphocyte activation markers (CCR5, HLA-DR, CD25, CD38 and CD71) were determined. Non parametric statistics were used to describe differences in the variables between the subgroups. RESULTS: Helminth prevalence ranged between 40%-60%. Four distinct subgroups of were identified, and this included egg positive/high Ascaris-specific IgE (egg(+)IgE(hi)), egg positive/low IgE (egg(+)IgE(lo)), egg negative/high IgE (egg(-)IgE(hi)) and egg negative/low IgE (egg(-)IgE(lo)) individuals. The egg(+)IgE(hi )subgroup displayed lymphocytopenia, eosinophilia, (low CD4(+ )counts in HIV(- )group), high viral load (in HIV(+ )group), and an activated lymphocyte profile. High Ascaris IgE subgroups (egg(+)IgE(hi )and egg(-)IgE(hi)) had eosinophilia, highest viral loads, and lower CD4(+ )counts in the HIV(- )group). Egg excretion and low IgE (egg(+)IgE(lo)) status demonstrated a modified Th(2 )immune profile with a relatively competent response to HIV. CONCLUSIONS: People with both helminth egg excretion and high Ascaris-IgE levels had dysregulated immune cells, high viral loads with more immune activation. A modified Th(2 )helminth response in individuals with egg positive stools and low Ascaris IgE showed a better HIV related immune profile. Future research on helminth-HIV co-infection should include parasite-specific IgE measurements in addition to coproscopy to delineate the different response phenotypes. Helminth infection affects the immune response to HIV in some individuals with high IgE and egg excretion in stool.
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spelling pubmed-32136742011-11-12 The influence of different helminth infection phenotypes on immune responses against HIV in co-infected adults in South Africa Mkhize-Kwitshana, Zilungile L Taylor, Myra Jooste, Pieter Mabaso, Musawenkosi LH Walzl, Gerhard BMC Infect Dis Research Article BACKGROUND: The convergent distribution of the Human Immunodeficiency Virus (HIV) and helminth infections has led to the suggestion that infection with helminths exacerbates the HIV epidemic in developing countries. In South Africa, it is estimated that 57% of the population lives in poverty and carries the highest burden of both HIV and helmith infections, however, the disease interactions are under-researched. METHODS: We employed both coproscopy and Ascaris lumbricoides-specific serum IgE to increase diagnostic sensitivity and to distinguish between different helminth infection phenotypes and their effects on immune responses in HIV co-infected individuals. Coproscopy was done by formol ether and Kato Katz methods. HIV positive and negative adults were stratified according to the presence or absence of A. lumbricoides and/or Trichuris trichuria eggs with or without elevated Ascaris IgE. Lymphocyte subsets were phenotyped by flow cytometry. Viral loads, serum total IgE and eosinophils were also analysed. Lymphocyte activation markers (CCR5, HLA-DR, CD25, CD38 and CD71) were determined. Non parametric statistics were used to describe differences in the variables between the subgroups. RESULTS: Helminth prevalence ranged between 40%-60%. Four distinct subgroups of were identified, and this included egg positive/high Ascaris-specific IgE (egg(+)IgE(hi)), egg positive/low IgE (egg(+)IgE(lo)), egg negative/high IgE (egg(-)IgE(hi)) and egg negative/low IgE (egg(-)IgE(lo)) individuals. The egg(+)IgE(hi )subgroup displayed lymphocytopenia, eosinophilia, (low CD4(+ )counts in HIV(- )group), high viral load (in HIV(+ )group), and an activated lymphocyte profile. High Ascaris IgE subgroups (egg(+)IgE(hi )and egg(-)IgE(hi)) had eosinophilia, highest viral loads, and lower CD4(+ )counts in the HIV(- )group). Egg excretion and low IgE (egg(+)IgE(lo)) status demonstrated a modified Th(2 )immune profile with a relatively competent response to HIV. CONCLUSIONS: People with both helminth egg excretion and high Ascaris-IgE levels had dysregulated immune cells, high viral loads with more immune activation. A modified Th(2 )helminth response in individuals with egg positive stools and low Ascaris IgE showed a better HIV related immune profile. Future research on helminth-HIV co-infection should include parasite-specific IgE measurements in addition to coproscopy to delineate the different response phenotypes. Helminth infection affects the immune response to HIV in some individuals with high IgE and egg excretion in stool. BioMed Central 2011-10-14 /pmc/articles/PMC3213674/ /pubmed/21999928 http://dx.doi.org/10.1186/1471-2334-11-273 Text en Copyright ©2011 Mkhize-Kwitshana et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mkhize-Kwitshana, Zilungile L
Taylor, Myra
Jooste, Pieter
Mabaso, Musawenkosi LH
Walzl, Gerhard
The influence of different helminth infection phenotypes on immune responses against HIV in co-infected adults in South Africa
title The influence of different helminth infection phenotypes on immune responses against HIV in co-infected adults in South Africa
title_full The influence of different helminth infection phenotypes on immune responses against HIV in co-infected adults in South Africa
title_fullStr The influence of different helminth infection phenotypes on immune responses against HIV in co-infected adults in South Africa
title_full_unstemmed The influence of different helminth infection phenotypes on immune responses against HIV in co-infected adults in South Africa
title_short The influence of different helminth infection phenotypes on immune responses against HIV in co-infected adults in South Africa
title_sort influence of different helminth infection phenotypes on immune responses against hiv in co-infected adults in south africa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213674/
https://www.ncbi.nlm.nih.gov/pubmed/21999928
http://dx.doi.org/10.1186/1471-2334-11-273
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